Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_assertion description "[Here we report a secondary reduction in calpain 3 expression in eight out of 16 patients with a primary dysferlinopathy and clinical features characteristic of limb girdle muscular dystrophy type 2B or Miyoshi myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_assertion evidence source_evidence_literature NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_assertion SIO_000772 11053681 NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_assertion wasDerivedFrom befree-20150227 NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_assertion wasGeneratedBy ECO_0000203 NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP280401.RAmlV8nB8sqwCCfhAa9jnSnvWGFf9z3iz5jol77kbaxhw130_provenance.